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Digitale Medien

Progression in nemaline myopathy (1989)

Nonaka, I. ; Ishiura, S. ; Arahata, K. ; [weitere]

Springer

Acta neuropathologica 78 (1989), S. 484-491

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Details

ISSN: 1432-0533

Schlagwort(e): Nemaline myopathy ; Lysosomal enzymes ; Acid phosphatase ; Cathepsins ; Myofibrillar degeneration

Quelle: Springer Online Journal Archives 1860-2000

Thema: Medizin

Notizen: Summary Four of seven patients with nemaline myopathy had severe, rapidly progressing symptoms. These four showed an increase in acid phosphatase activity in muscle fibers demonstrated by histochemistry and cathepsin B&L activity by biochemical measurement. On electron microscopy, nemaline bodies, occasionally disorganized myofibrils and autophagic vacuoles containing sarcoplasmic debris and glycogen particles were seen. Focal myofibrillar degeneration, through an unknown pathogenetic mechanism, induces an increase in lysosomal enzymes in the skeletal muscles which may be closely correlated with a rapid aggravation of muscle weakness in nemaline myopathy.

Materialart: Digitale Medien

URL: http://dx.doi.org/10.1007/BF00687709

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